ENST00000334504.12:c.4835G>T
MANE Select
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ENSP00000334733.7:p.Gly1612Val
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ENST00000334504.11:c.4835G>T
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ENSP00000334733.7:p.Gly1612Val
|
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ENST00000372216.8:c.4838G>T
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ENSP00000361290.4:p.Gly1613Val
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ENST00000394872.6:c.4886G>T
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ENSP00000378340.3:p.Gly1629Val
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ENST00000538570.5:c.4664G>T
|
ENSP00000445236.1:p.Gly1555Val
|
|
ENST00000545689.2:c.4799G>T
|
ENSP00000443707.2:p.Gly1600Val
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ENST00000621266.4:c.4763G>T
|
ENSP00000482970.1:p.Gly1588Val
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NM_001287758.1:c.4886G>T
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NP_001274687.1:p.Gly1629Val
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NM_001287759.1:c.4763G>T
|
NP_001274688.1:p.Gly1588Val
|
|
NM_001287760.1:c.4664G>T
|
NP_001274689.1:p.Gly1555Val
|
|
NM_001847.3:c.4838G>T
|
NP_001838.2:p.Gly1613Val
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NM_033641.3:c.4835G>T
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NP_378667.1:p.Gly1612Val
|
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XM_006724617.2:c.4889G>T
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XP_006724680.1:p.Gly1630Val
|
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XM_011530852.1:c.4817G>T
|
XP_011529154.1:p.Gly1606Val
|
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XM_011530853.1:c.4805G>T
|
XP_011529155.1:p.Gly1602Val
|
|
XM_006724617.3:c.4889G>T
|
XP_006724680.1:p.Gly1630Val
|
|
XM_011530852.2:c.4817G>T
|
XP_011529154.1:p.Gly1606Val
|
|
XM_011530853.3:c.4805G>T
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XP_011529155.1:p.Gly1602Val
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NM_001847.4:c.4838G>T
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NP_001838.2:p.Gly1613Val
|
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NM_033641.4:c.4835G>T
MANE Select
|
NP_378667.1:p.Gly1612Val
|
|
NM_001287758.2:c.4886G>T
|
NP_001274687.1:p.Gly1629Val
|
|
NM_001287759.2:c.4763G>T
|
NP_001274688.1:p.Gly1588Val
|
|
NM_001287760.2:c.4664G>T
|
NP_001274689.1:p.Gly1555Val
|
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